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Accurate diagnosis of cicatricial alopecias requires thorough scalp examination and multiple biopsy techniques.

Pregnancy can cause skin changes and conditions that need correct diagnosis and treatment for the health of the mother and baby.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Understanding where cancer cells come from helps create better prevention and treatment methods.

More dermal papilla cells in hair follicles lead to larger, healthier hair, while fewer cells cause hair thinning and loss.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Pannexin 3 is important for bone formation and the development of bone cells.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Some stem cells in the body rarely divide, which could help create better treatments for diseases and aging.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Certain zinc transporters are essential for healthy skin and managing zinc in the body could help treat skin problems.

Mild essential fatty acid deficiency can cause health issues and is worsened by low-fat diets.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.